Neuronopathy, distal hereditary motor, autosomal dominant

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Subtype of: Distal hereditary motor neuropathy · Neuronopathy, distal hereditary motor
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
neuronopathy, distal hereditary motor, autosomal dominant
MONDO_0030860MONDO_0011879MONDO_0859300MONDO_0015353MONDO_0012080MONDO_0008025MONDO_0013884MONDO_0957875
BSCL2 Unknown
17663003 14981520 18585921 21533227 24604904
Open Targets —
DCTN1 Unknown
19279216 12627231 19136952 22777741 16505168
Open Targets
EMILIN1 Unknown
38963291 31978608 26462740
Open Targets
GARS1 Unknown
23279345 24627108 12690580 26503042 17035524 25168514 17545306 17101916
Open Targets
HSPB1 Unknown
25965061 20178975 28144995 20870250 15122254 23643870 23948568 22176143 23728742 18952241 18832141
Open Targets
HSPB8 Unknown
15122253 15565283 28144995
ClinGen, Open Targets
REEP1 Unknown
22703882
Open Targets
SPTAN1 Unknown
32811770 22258530 20493457
Open Targets
All9 Causal1 Unknown8
Related Diseases Diseases that share the most curated genes with Neuronopathy, distal hereditary motor, autosomal dominant.
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Distal axonal motor neuropathy-myofibrillar myopathy syndrome 1 shared geneHSPB8 Related via 1 shared gene including HSPB8. Vacuolar myopathy 1 shared geneHSPB8 Related via 1 shared gene including HSPB8. Distal muscular dystrophy 1 shared geneHSPB8 Related via 1 shared gene including HSPB8. Distal spinal muscular atrophy 1 shared geneHSPB8 Related via 1 shared gene including HSPB8. Distal hereditary motor neuropathy 1 shared geneHSPB8 Related via 1 shared gene including HSPB8.